Canonical Allele Identifier: CA368367577

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99358459G>T (hg19) ; chr7:g.99760836G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760836G>T , CM000669.2:g.99760836G>T	GRCh38
NC_000007.13:g.99358459G>T , CM000669.1:g.99358459G>T	GRCh37
NC_000007.12:g.99196395G>T	NCBI36
NG_008421.1:g.28350C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1492C>A	ENSP00000337915.3:p.Pro498Thr
ENST00000651162.1:n.834C>A
ENST00000651514.1:c.1399C>A MANE Select	ENSP00000498939.1:p.Pro467Thr
ENST00000651783.1:c.940C>A	ENSP00000498924.1:p.Pro314Thr
ENST00000652018.1:c.1252C>A	ENSP00000498733.1:p.Pro418Thr
ENST00000336411.6:c.1399C>A	ENSP00000337915.2:p.Pro467Thr
ENST00000354593.6:c.949C>A	ENSP00000346607.2:p.Pro317Thr
NM_001202855.2:c.1396C>A	NP_001189784.1:p.Pro466Thr
NM_017460.5:c.1399C>A	NP_059488.2:p.Pro467Thr
XM_011515841.1:c.1492C>A	XP_011514143.1:p.Pro498Thr
XM_011515842.1:c.1489C>A	XP_011514144.1:p.Pro497Thr
NM_017460.6:c.1399C>A MANE Select	NP_059488.2:p.Pro467Thr
NM_001202855.3:c.1396C>A	NP_001189784.1:p.Pro466Thr